Canonical Allele Identifier: CA1358881721
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263232T= , CM000665.2:g.39263232T= GRCh38
NC_000003.11:g.39304723T= , CM000665.1:g.39304723T= GRCh37
NC_000003.10:g.39279727T= NCBI36
NG_016362.1:g.23504A=

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2749T=